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  2. Morphine - Wikipedia

    en.wikipedia.org/wiki/Morphine

    Morphine is highly addictive and prone to abuse. [12] If one's dose is reduced after long-term use, opioid withdrawal symptoms may occur. [12] Caution is advised for the use of morphine during pregnancy or breastfeeding, as it may affect the health of the baby. [12] [2] Morphine was first isolated in 1804 by German pharmacist Friedrich Sertürner.

  3. Patient-controlled analgesia - Wikipedia

    en.wikipedia.org/wiki/Patient-controlled_analgesia

    "A comparison of morphine administered by patient-controlled analgesia and regularly scheduled intramuscular injection in severe, postoperative pain". Journal of Pain and Symptom Management. 3 (1): 15– 22. doi: 10.1016/0885-3924(88)90133-9. PMID 3351344. Sechzer PH (1971). "Studies in pain with the analgesic-demand system". Anesthesia and ...

  4. Opioid-induced hyperalgesia - Wikipedia

    en.wikipedia.org/wiki/Opioid-induced_hyperalgesia

    Opioid-induced hyperalgesia (OIH) or opioid-induced abnormal pain sensitivity, also called paradoxical hyperalgesia, is an uncommon condition of generalized pain caused by the long-term use of high dosages of opioids [1] such as morphine, [2] oxycodone, [3] and methadone.

  5. Intrathecal administration - Wikipedia

    en.wikipedia.org/wiki/Intrathecal_administration

    The use of intrathecal morphine may be limited by severe pruritus and urinary retention. [citation needed] Pethidine has the unusual property of being both a local anaesthetic and opioid analgesic, which occasionally permits its use as the sole intrathecal anaesthetic agent. [citation needed]

  6. Hydromorphone - Wikipedia

    en.wikipedia.org/wiki/Hydromorphone

    Hydromorphone is extensively metabolized in the liver to hydromorphone-3-glucuronide, which has no analgesic effects. As similarly seen with the morphine metabolite, morphine-3-glucuronide, a build-up in levels of hydromorphone-3-glucuronide may produce excitatory neurotoxic effects such as restlessness, myoclonus and hyperalgesia. Patients ...

  7. Nicomorphine - Wikipedia

    en.wikipedia.org/wiki/Nicomorphine

    The 3,6-diesters of morphine are drugs with more rapid and complete central nervous system penetration due to increased lipid solubility and other structural considerations. The prototype for this subgroup of semi-synthetic opiates is heroin and the group also includes dipropanoylmorphine, diacetyldihydromorphine, disalicylmorphine and others.

  8. Pharmacist took morphine meant for suffering patients ... - AOL

    www.aol.com/news/pharmacist-took-morphine-meant...

    Federal authorities say a Minnesota pharmacist took morphine from the “stock bottle” meant to fulfill patient prescriptions and replaced the missing liquid with water.. In doing so, the 42 ...

  9. Morphine - Wikipedia

    en.wikipedia.org/wiki/(+)-Morphine

    To the contrary, in rats, (+)-morphine acts as an antianalgesic and is approximately 71,000 times more potent as an antianalgesic than (−)-morphine is as an analgesic. [ 1 ] (+)-Morphine derives its antianalgesic effects by being a selective-agonist of the Toll-like receptor 4 (TLR4), which due to not binding to opioid receptors allows it to ...